1. Gene
  2. EIF3G - eukaryotic translation initiation factor 3 subunit G Gene

EIF3G - eukaryotic translation initiation factor 3 subunit G Gene

Homo sapiens

Also known as EIF3S4; EIF3-P42; eIF3-p44; eIF3-delta

Gene ID: 8666 | Gene type: protein coding

About EIF3G

Cytogenetic location: 19p13.2 Genomic coordinates (GRCh38): 19:10,115,014-10,119,899 (from NCBI)

This gene has 15 transcripts (splice variants) and 209 orthologues. Ubiquitous expression in ovary (RPKM 90.1), testis (RPKM 63.4) and 25 other tissues.

Summary

This gene encodes a core subunit of the eukaryotic translation initiation factor 3 (eIF3) complex, which is required for initiation of protein translation. An N-terminal Caspase cleavage product of the encoded protein may stimulate degradation of DNA. A mutation in this gene is associated with narcolepsy. [provided by RefSeq, Jul 2016]

EIF3G Products(1)

mRNA Protein Name
NM_003755.5 NP_003746.2 eukaryotic translation initiation factor 3 subunit G

EIF3G Protein Structure

eIF3g

eIF3g: Eukaryotic translation initiation factor 3 subunit G (54 - 175)

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (241 - 303)

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Protein Preferred Names Protein Names

eukaryotic translation initiation factor 3 subunit G

eukaryotic translation initiation factor 3 RNA-binding subunit

Recombinant EIF3G Proteins

Cat. No. Product Name Accession Purity
HY-P700506 EIF3G Protein, Human (His-SUMO) O75821 (P2-N320) ≥95%

Related Diseases

Diseases Alias
Narcolepsy

Paroxysmal Sleep

Gelineau Syndrome

Narcoleptic Syndrome

Narcolepsy-Cataplexy Syndrome

Cataplexy And Narcolepsy

Narcolepsy, Without Cataplexy

Gelineau'S Syndrome

Narcolepsy With Or Without Cataplexy

Narcolepsy Nos

Cardiomyopathy, Familial Hypertrophic, 15

Hypertrophic Cardiomyopathy 15

CMH15

Cardiomyopathy, Hypertrophic, 15

Cardiomyopathy Familial Hypertrophic 15

Cardiomyopathy, Familial Hypertrophic 15

Cardiomyopathy, Hypertrophic, Familial, Type 15

Craniotubular Dysplasia, Ikegawa Type

CTDI

Craniotubular Dysplasia Ikegawa Type

Doid:0112340

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus EIF3G RGD RGD:1307191
Canis familiaris EIF3G VGNC VGNC:40273
Bos taurus EIF3G VGNC VGNC:28397
Macaca mulatta EIF3G VGNC VGNC:72190
Felis catus EIF3G VGNC VGNC:61783
Mus musculus EIF3G MGD MGI:1858258
Others EIF3G NCBI